Search

everythinglearnresearchcommunity

for

Search:↓

Low vitamin D levels are common in people with Alopecia Areata.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Topical diphencyprone helped regrow hair in mice and rats with a condition similar to human hair loss.

Special and immunohistochemical stains are not routinely needed for diagnosing hair disorders.

People with alopecia areata may be more likely to have a certain type of hearing loss.

Greying hairs may be protected from alopecia areata.

The conditions alopecia areata, primary sclerosing cholangitis, and ulcerative colitis may be linked by shared autoimmune and cell death mechanisms.

Frontal fibrosing alopecia may be linked to genital Lichen sclerosus through an autoimmune process.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Higher DKK-1 levels found in hair loss patients; L-ascorbic acid 2-phosphate, L-threonate, and ginsenoside F2 may help promote hair growth.

Red light at 627 nm can safely trigger IL-4 release in skin cells, potentially helping treat inflammatory skin conditions.

A gluten-free diet stopped a child's hair-eating behavior and suggested she had celiac disease.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

The article concludes that different types of hair loss require specific treatments and psychological support is important.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The study concluded that combination therapy with topical corticosteroids and hydroxychloroquine or finasteride is effective in treating Frontal fibrosing alopecia in Asians.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

The girl's regrown brown hair had less of certain pigments than her original black hair.

AGA linked to inflammation, stress, fibrosis, and disturbed hair follicle stem cells.

Certain gene variations increase the risk of alopecia areata in Koreans.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Children with autoimmune gastritis showed improved intestinal health over time and should be checked for other autoimmune conditions.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Transplanting growing hair follicles into scars can help regenerate and improve scar tissue.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

The Alopecia Areata Assessment Tool (ALTO) effectively identifies alopecia areata from other hair loss types but needs more validation.